Clinical Site Budgets Manager

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Join to apply for the Clinical Site Budgets Manager role at Blueprint Medicines

This range is provided by Blueprint Medicines. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$60.00/hr - $60.00/hr

Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe.

Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors.

Job Title:
Clinical Site Budgets Manager

Location:
Remote (EST Hours)



Job Description

How will your role help us transform hope into reality?

This position reports into the Senior Manager Clinical Site Budgets.

The right candidate will possess an understanding of Investigator Grant Management activities for successful execution of multiple clinical trials primarily in oncology, allergy and hematology indications in various phases of development.

Responsibilities of this position involve the day-to-day management of overseeing the CROs development of investigator payments, reviewing investigator grant budgets and developing parameters for negotiations for the CRO. Will act as an escalation point for the CRO and the investigator when budgets fall out the acceptable range.

What will you do?

• Review investigator budgets against the schedule of events within the protocol
• Identify research related costs versus Standard of Care costs and support teams in site contract negotiations
• Use Fair Market Value (FMV) benchmarking tools such as Grant Plan and Grants Manager to develop template study site budgets
• Leads and oversees the overall investigator site payment process with the CROs
• Establish acceptable negotiation ranges for our CROs to use when working with investigators
• Serve as an escalation point for the CRO for Investigator Grant Negotiations with sites
• Act as SME for internal clients regarding FMV costs and investigator reimbursement.
• Supervises the status of budget negotiation to expected timeline and reviews CRO metrics of performance
• Identifies and seeks efficiency with our CROs, to ensure improved value for service
• Participates and could present in Clinical Trial, CRO kick off, Investigator budget financial review and CRO governance meetings

• Minimum
  
  Education Required:
  
  Bachelor’s degree in scientific or business discipline.
• Previous clinical experience a plus
• Understanding of the drug development process T
• The candidate should ideally have 3 + years in investigator budget and contract management with a sponsor company or CRO managing various phase clinical trials.
• Ability to work with minimal direction
• Motivated self-starter who can work in a fast-paced environment
• Creative problem solver with good communication and written skills.
• Strong interpersonal and organizational skills are needed, with a high degree of attention to detail.
• Proficient with the MS…